ZipRecruiter

Log In

1

Associate Director Of Clinical Research Jobs (NOW HIRING)

Frontage Laboratories

Clinical Research Nurse

Secaucus, NJ · On-site

$45 - $55/hr

... of the Principal Investigator and Sub-Investigators, Director, Associate Director, and Clinical Research Coordinators. * Record study data in the source documents. Evaluate and review study data to ...

previous pagenext page

Showing results 21-40

All JobsAssociate Of Clinical Research JobsAssociate Director Of Clinical Research Jobs

Associate Director Of Clinical Research information

See salary details

$28.5K

$115.2K

$243K

How much do associate director of clinical research jobs pay per year?

As of Aug 7, 2026, the average yearly pay for associate director of clinical research in the United States is $115,163.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $147,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as an associate director of clinical research?

To thrive as an Associate Director of Clinical Research, you need advanced knowledge of clinical trial design, regulatory compliance, and project management, usually supported by a degree in life sciences or a related field and significant clinical research experience. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) guidelines, and certifications such as CCRA or CCRP are typically expected. Leadership, strategic thinking, and strong interpersonal skills help drive cross-functional teams and effective stakeholder communication. These combined skills ensure trials are conducted efficiently, ethically, and in accordance with regulatory standards, which is critical for successful research outcomes.

What does an associate director of clinical research do?

An Associate Director of Clinical Research oversees the planning, execution, and management of clinical trials and research studies within a healthcare or pharmaceutical organization. They ensure that studies comply with regulatory requirements, company policies, and ethical standards. This role involves managing teams, collaborating with various departments, and analyzing data to support new drug development or medical procedures. They also contribute to strategic decision-making and the improvement of clinical trial processes.

How does an associate director of clinical research collaborate with cross-functional teams during a clinical trial?

An Associate Director of Clinical Research plays a central role in coordinating with various teams such as regulatory affairs, data management, biostatistics, and clinical operations. They ensure that study protocols are followed, timelines are met, and communication between departments is seamless. Regular meetings, progress updates, and collaborative problem-solving are key aspects of their daily routine. This cross-functional teamwork helps to address challenges efficiently and ensures that clinical trials run smoothly from start to finish.

What is the difference between Associate Director Of Clinical Research vs Clinical Project Manager?

AspectAssociate Director Of Clinical ResearchClinical Project Manager
CredentialsTypically requires a master's or doctoral degree in life sciences, along with experience in clinical research.Usually requires a bachelor's or master's degree in a related field, with relevant project management experience.
Work EnvironmentWorks in pharmaceutical or biotech companies, overseeing multiple clinical trials and teams.Manages specific clinical projects, coordinating activities between teams and vendors.
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and CROs, focusing on research oversight.Found in similar settings, focusing on project execution and timelines.

The Associate Director Of Clinical Research typically holds a higher-level role with broader oversight responsibilities compared to a Clinical Project Manager, who focuses on managing individual clinical projects. Both roles require relevant experience and credentials but differ mainly in scope and seniority.

More about Associate Director Of Clinical Research jobs
What cities are hiring for Associate Director Of Clinical Research jobs? Cities with the most Associate Director Of Clinical Research job openings:
What states have the most Associate Director Of Clinical Research jobs? States with the most job openings for Associate Director Of Clinical Research jobs include:
What job categories do people searching Associate Director Of Clinical Research jobs look for? The top searched job categories for Associate Director Of Clinical Research jobs are:
Associate Director Of Clinical Research jobs near you
Infographic showing various Associate Director Of Clinical Research job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $115,163 per year, or $55.4 per hour.

Regional Director of Clinical Operations

Tekton Research Inc

Edmond, OK • On-site

Full-time

Posted yesterday

New

Job description

Regional Director of Clinical Operations - Oklahoma and Kansas

Position Type: Full-Time | Exempt

Position Summary:

Tekton Research is seeking an experienced Regional Director of Clinical Operations to oversee operational performance, revenue growth, and quality execution across clinical research sites. This strategic leadership role is responsible for ensuring sites achieve key performance indicators (KPIs), meet revenue objectives, maintain compliance with study requirements, and successfully execute clinical trials.

The Regional Director of Clinical Operations serves as a key partner to site leadership, managers, and Principal Investigators (PIs), providing guidance, identifying business risks, implementing solutions, and reporting performance updates to executive leadership.

Reports To: Senior Regional Director of Clinical Operations / Chief Operating Officer (COO)

Essential Responsibilities:
  • Monitor and evaluate study startup performance to support successful trial activation, revenue generation, and future business growth.
  • Assess site revenue performance and provide strategic recommendations to achieve financial goals.
  • Hold sites accountable for appropriate scheduling, recruitment strategies, and operational execution to meet or exceed recruitment and revenue targets.
  • Provide oversight to ensure sites are appropriately staffed, trained, and prepared to meet study conduct requirements.
  • Ensure sites maintain appropriate resources, equipment, and operational readiness for successful study execution.
  • Monitor site compliance with contractual requirements, including completion of study visits, EDC entry, query resolution, and required documentation.
  • Serve as a clinical research resource to support sites with operational and study-related questions.
  • Ensure sites are conducting quality control activities and partner with Quality Assurance (QA) as needed for audits, inspections, and quality initiatives.
  • Collaborate with site managers and Principal Investigators to ensure appropriate investigator coverage and study support.
  • Communicate site goals, expectations, and performance metrics with managers and investigators.
  • Track and report site performance, progress, challenges, and business risks to the Executive Director and/or COO.
  • Develop and implement solutions to mitigate operational and business risks.
  • Perform other duties as assigned.
Required Knowledge, Skills, and Abilities:

Successful candidates will have demonstrated expertise in:

  • Clinical research operations and study management
  • Regulatory requirements and compliance
  • Clinical procedures and trial execution
  • Sponsor communication and relationship management
  • Project management principles
  • Human resources and team leadership practices
  • Operational performance management and KPI oversight
Education and Experience:
  • Bachelor’s degree, specialized degree, or equivalent relevant education and experience preferred.
  • 7–10 years of experience in the clinical research industry.
  • 5+ years of experience in a supervisory or management leadership role.
  • Proven experience managing clinical research operations, site performance, and cross-functional teams.
Physical Requirements:
  • Ability to work extended periods at a desk and on a computer.
  • Ability to occasionally lift up to 15 pounds.
  • Willingness and ability to travel, including air travel, to support sites within the Oklahoma and Kansas region.
Why Join Tekton Research?

At Tekton Research, we are committed to advancing clinical research through operational excellence, quality patient care, and strong partnerships with sponsors, investigators, and research teams. The Regional Director of Clinical Operations plays a critical role in driving site success and supporting the delivery of high-quality clinical trials.